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Acute myeloid leukemia with monosomy 7 ectopic virus integration site-1 overexpression and central diabetes insipidus: A case report

机译:急性髓样白血病伴单核7异位病毒整合位点1过表达和中枢性尿崩症:一例报告

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摘要

Central diabetes insipidus (DI) is a rare complication in patients with acute myeloid leukemia (AML), typically occurring in patients with abnormalities of chromosomes 3 or 7. The association between AML with monosomy 7 and DI has been described in a number of studies; however, DI has been rarely reported in cases of ectopic virus integration site-1 (EVI1)-positive AML with monosomy 7. The current study reports a case of AML with monosomy 7 and EVI1 overexpression, with central DI as the initial symptom. The patient was an 18-year-old female who presented with polyuria and polydipsia. Bone marrow aspiration revealed 83.5% myeloperoxidase-positive blasts without trilineage myelodysplasia. The karyotype was 45,XX,-7, and the patient presented monosomy 7 and EVI1 overexpression (−7/EVI1+) without 3q aberration. Treatment with induction therapy was unsuccessful. To the best of our knowledge, this is the second case of DI-AML with -7/EVI1+ and without a 3q aberration. The possible mechanisms associated with EVI1, monosomy 7 and DI were investigated.
机译:中枢性尿崩症(DI)是急性髓细胞性白血病(AML)患者的罕见并发症,通常发生在3号或7号染色体异常的患者中。AML与7号单体性病和DI的相关性已在许多研究中进行了描述。但是,在异位病毒整合位点1(EVI1)阳性AML并带有7号单体性的情况下,很少报道有DI。目前的研究报道了7号单体性和EVI1过表达的AML病例,其中以中枢DI为主要症状。该患者是一名18岁女性,患有多尿和多饮。骨髓抽吸显示83.5%的髓过氧化物酶阳性胚泡,无三系性骨髓增生异常。核型为45,XX,-7,患者出现7号单体性和EVI1过表达(-7 / EVI1 + ),而没有3q像差。诱导疗法治疗失败。据我们所知,这是第二例具有-7 / EVI1 + 且没有3q像差的DI-AML。研究了与EVI1、7号单体和DI相关的可能机制。

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